METRONIDazole Injection, USP 500 mg (5 mg/mL) in 100 mL Single Dose Flexible Container, Rx only, For IV Use, Hospira Inc., Lake Forest, IL --- NDC 0409-7811-24
Recall Number: D-0480-2017
Firm: Hospira Inc., A Pfizer Company
Classification: Class II
Status: Terminated
Report Date: 20170301
Initiation Date: 20170210
Termination Date: 20190403
Reason for Recall
Lack of Sterility Assurance: customer report of leaking bag
Product Description
METRONIDazole Injection, USP 500 mg (5 mg/mL) in 100 mL Single Dose Flexible Container, Rx only, For IV Use, Hospira Inc., Lake Forest, IL --- NDC 0409-7811-24